LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
Disease: Obesity ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11208659
rs11208659
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0028754
Disease:
Obesity 		C 0.800 GeneticVariation GWASDB Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. 23563609 2013
dbSNP: rs11208659
rs11208659
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0028754
Disease:
Obesity 		C 0.800 GeneticVariation GWASCAT Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. 23563609 2013